Rgs12 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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165 records found for search term Rgs12

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405715419	CV3309179	single nucleotide variant	NM_001394154.1(RGS12):c.65G>A (p.Ser22Asn)	not specified [RCV004449118]	uncertain significance	4	3316235	3316235	Human		name
405715439	CV3309181	single nucleotide variant	NM_001394154.1(RGS12):c.80G>A (p.Arg27Gln)	not specified [RCV004449120]	uncertain significance	4	3316250	3316250	Human		name
407460462	CV3472800	single nucleotide variant	NM_001394154.1(RGS12):c.44C>T (p.Pro15Leu)	not specified [RCV004658460]	uncertain significance	4	3316214	3316214	Human		name
407474244	CV3472810	single nucleotide variant	NM_001394154.1(RGS12):c.61C>T (p.Arg21Trp)	not specified [RCV004662949]	uncertain significance	4	3316231	3316231	Human		name
597788000	CV3586295	single nucleotide variant	NM_001394154.1(RGS12):c.28C>T (p.Arg10Cys)	not specified [RCV004855382]	uncertain significance	4	3316198	3316198	Human		name
597775676	CV3586297	single nucleotide variant	NM_001394154.1(RGS12):c.89C>T (p.Ala30Val)	not specified [RCV004852312]	uncertain significance	4	3316259	3316259	Human		name
597788031	CV3586313	single nucleotide variant	NM_001394154.1(RGS12):c.56G>A (p.Arg19Lys)	not specified [RCV004855390]	uncertain significance	4	3316226	3316226	Human		name
401927864	CV2822365	single nucleotide variant	NM_001394154.1(RGS12):c.2400A>G (p.Pro800=)	not provided [RCV003439220]	likely benign	4	3416094	3416094	Human		name
401923203	CV2822366	single nucleotide variant	NM_001394154.1(RGS12):c.2745C>T (p.His915=)	not provided [RCV003434950]	likely benign	4	3417525	3417525	Human		name
597788026	CV3586310	single nucleotide variant	NM_001394154.1(RGS12):c.244A>G (p.Lys82Glu)	not specified [RCV004855389]	uncertain significance	4	3316414	3316414	Human		name
15196379	CV698496	single nucleotide variant	NM_001394154.1(RGS12):c.2502G>A (p.Ala834=)	not provided [RCV000956176]	benign	4	3416987	3416987	Human		name
8631159	CV86315	single nucleotide variant	NM_198229.2(RGS12):c.3556G>A (p.Glu1186Lys)	Malignant melanoma [RCV000066406]	not provided	4	3428702	3428702	Human		name
156401789	CV2217754	single nucleotide variant	NM_001394154.1(RGS12):c.994G>A (p.Ala332Thr)	not specified [RCV004083934]	uncertain significance	4	3317164	3317164	Human		name
156330260	CV2226969	single nucleotide variant	NM_001394154.1(RGS12):c.910G>A (p.Val304Met)	not specified [RCV004097365]	uncertain significance	4	3317080	3317080	Human		name
155906024	CV2303229	single nucleotide variant	NM_001394154.1(RGS12):c.874G>A (p.Ala292Thr)	not specified [RCV004156984]	uncertain significance	4	3317044	3317044	Human		name
156164899	CV2319819	single nucleotide variant	NM_001394154.1(RGS12):c.686C>T (p.Ala229Val)	not specified [RCV004165880]	uncertain significance	4	3316856	3316856	Human		name
156265641	CV2389082	single nucleotide variant	NM_001394154.1(RGS12):c.949A>G (p.Met317Val)	not specified [RCV004235420]	uncertain significance	4	3317119	3317119	Human		name
329392940	CV2449391	single nucleotide variant	NM_001394154.1(RGS12):c.611A>T (p.His204Leu)	not specified [RCV004266551]	uncertain significance	4	3316781	3316781	Human		name
401866910	CV2769745	single nucleotide variant	NM_001394154.1(RGS12):c.304T>C (p.Phe102Leu)	not specified [RCV004351662]	likely benign	4	3316474	3316474	Human		name
405715291	CV3309160	single nucleotide variant	NM_001394154.1(RGS12):c.298G>A (p.Gly100Ser)	not specified [RCV004449099]	uncertain significance	4	3316468	3316468	Human		name
405715306	CV3309162	single nucleotide variant	NM_001394154.1(RGS12):c.319A>T (p.Ser107Cys)	not specified [RCV004449101]	uncertain significance	4	3316489	3316489	Human		name
405715318	CV3309164	single nucleotide variant	NM_001394154.1(RGS12):c.327A>C (p.Glu109Asp)	not specified [RCV004449103]	uncertain significance	4	3316497	3316497	Human		name
405715326	CV3309165	single nucleotide variant	NM_001394154.1(RGS12):c.341A>G (p.Tyr114Cys)	not specified [RCV004449104]	uncertain significance	4	3316511	3316511	Human		name
405715407	CV3309177	single nucleotide variant	NM_001394154.1(RGS12):c.604G>A (p.Val202Ile)	not specified [RCV004449116]	uncertain significance	4	3316774	3316774	Human		name
405715413	CV3309178	single nucleotide variant	NM_001394154.1(RGS12):c.605T>C (p.Val202Ala)	not specified [RCV004449117]	uncertain significance	4	3316775	3316775	Human		name
405715430	CV3309180	single nucleotide variant	NM_001394154.1(RGS12):c.734C>G (p.Ser245Cys)	not specified [RCV004449119]	likely benign	4	3316904	3316904	Human		name
405715446	CV3309182	single nucleotide variant	NM_001394154.1(RGS12):c.917C>T (p.Pro306Leu)	not specified [RCV004449121]	uncertain significance	4	3317087	3317087	Human		name
405715451	CV3309183	single nucleotide variant	NM_001394154.1(RGS12):c.967G>A (p.Gly323Arg)	not specified [RCV004449122]	uncertain significance	4	3317137	3317137	Human		name
407460453	CV3472794	single nucleotide variant	NM_001394154.1(RGS12):c.956C>T (p.Thr319Met)	not specified [RCV004658458]	uncertain significance	4	3317126	3317126	Human		name
407508085	CV3472798	single nucleotide variant	NM_001394154.1(RGS12):c.925C>T (p.Arg309Trp)	not specified [RCV004671931]	uncertain significance	4	3317095	3317095	Human		name
407474208	CV3472801	single nucleotide variant	NM_001394154.1(RGS12):c.778C>T (p.Arg260Trp)	not specified [RCV004662941]	uncertain significance	4	3316948	3316948	Human		name
597787992	CV3586291	single nucleotide variant	NM_001394154.1(RGS12):c.521C>T (p.Ser174Leu)	not specified [RCV004855380]	uncertain significance	4	3316691	3316691	Human		name
597775683	CV3586301	single nucleotide variant	NM_001394154.1(RGS12):c.995C>A (p.Ala332Asp)	not specified [RCV004852314]	uncertain significance	4	3317165	3317165	Human		name
597775687	CV3586302	single nucleotide variant	NM_001394154.1(RGS12):c.590A>C (p.Glu197Ala)	not specified [RCV004852315]	uncertain significance	4	3316760	3316760	Human		name
597788014	CV3586303	single nucleotide variant	NM_001394154.1(RGS12):c.746C>T (p.Ser249Phe)	not specified [RCV004855386]	uncertain significance	4	3316916	3316916	Human		name
597775691	CV3586304	single nucleotide variant	NM_001394154.1(RGS12):c.989A>G (p.Glu330Gly)	not specified [RCV004852316]	uncertain significance	4	3317159	3317159	Human		name
597788043	CV3586316	single nucleotide variant	NM_001394154.1(RGS12):c.611A>G (p.His204Arg)	not specified [RCV004855393]	uncertain significance	4	3316781	3316781	Human		name
598188834	CV3902538	single nucleotide variant	NM_001394154.1(RGS12):c.964G>A (p.Asp322Asn)	not specified [RCV005266632]	uncertain significance	4	3317134	3317134	Human		name
598188849	CV3902540	single nucleotide variant	NM_001394154.1(RGS12):c.349A>G (p.Lys117Glu)	not specified [RCV005266634]	uncertain significance	4	3316519	3316519	Human		name
598188870	CV3902543	single nucleotide variant	NM_001394154.1(RGS12):c.446T>A (p.Met149Lys)	not specified [RCV005266637]	uncertain significance	4	3316616	3316616	Human		name
15189811	CV720949	single nucleotide variant	NM_001394154.1(RGS12):c.963C>G (p.Asp321Glu)	not provided [RCV000887926]	likely benign	4	3317133	3317133	Human		name
15099254	CV748923	single nucleotide variant	NM_001394154.1(RGS12):c.3825G>A (p.Pro1275=)	not provided [RCV000914423]	likely benign	4	3430666	3430666	Human		name
15185801	CV764451	single nucleotide variant	NM_001394154.1(RGS12):c.4191C>T (p.Pro1397=)	not provided [RCV000931164]	likely benign	4	3439531	3439531	Human		name
156365472	CV2193211	single nucleotide variant	NM_001394154.1(RGS12):c.1793C>G (p.Pro598Arg)	not specified [RCV004071201]	uncertain significance	4	3317963	3317963	Human		name
156170522	CV2197902	single nucleotide variant	NM_001394154.1(RGS12):c.1357G>A (p.Gly453Arg)	not specified [RCV004077125]	uncertain significance	4	3317527	3317527	Human		name
156376371	CV2210556	single nucleotide variant	NM_001394154.1(RGS12):c.1481G>C (p.Arg494Thr)	not specified [RCV004083364]	uncertain significance	4	3317651	3317651	Human		name
156212974	CV2257334	single nucleotide variant	NM_001394154.1(RGS12):c.1208G>A (p.Arg403His)	not specified [RCV004125431]	uncertain significance	4	3317378	3317378	Human		name
156032824	CV2259688	single nucleotide variant	NM_001394154.1(RGS12):c.1130C>T (p.Ala377Val)	not specified [RCV004116712]	uncertain significance	4	3317300	3317300	Human		name
155903239	CV2274843	single nucleotide variant	NM_001394154.1(RGS12):c.2572G>A (p.Gly858Ser)	not specified [RCV004133043]	likely benign	4	3417057	3417057	Human		name
155999584	CV2287282	single nucleotide variant	NM_001394154.1(RGS12):c.2768T>C (p.Leu923Pro)	not specified [RCV004146919]	uncertain significance	4	3420648	3420648	Human		name
156173660	CV2290137	single nucleotide variant	NM_001394154.1(RGS12):c.1273G>A (p.Gly425Ser)	not specified [RCV004152804]	uncertain significance	4	3317443	3317443	Human		name
155944491	CV2295164	single nucleotide variant	NM_001394154.1(RGS12):c.1115G>C (p.Cys372Ser)	not specified [RCV004158261]	uncertain significance	4	3317285	3317285	Human		name
156045320	CV2319006	single nucleotide variant	NM_001394154.1(RGS12):c.1035C>G (p.Asp345Glu)	not specified [RCV004178096]	uncertain significance	4	3317205	3317205	Human		name
156063633	CV2321092	single nucleotide variant	NM_001394154.1(RGS12):c.1172G>A (p.Arg391Gln)	not specified [RCV004174917]	uncertain significance	4	3317342	3317342	Human		name
155918931	CV2333099	single nucleotide variant	NM_001394154.1(RGS12):c.2386C>T (p.Arg796Cys)	not specified [RCV004194392]	uncertain significance	4	3416080	3416080	Human		name
156191979	CV2356918	single nucleotide variant	NM_001394154.1(RGS12):c.2525C>T (p.Pro842Leu)	not specified [RCV004204291]	uncertain significance	4	3417010	3417010	Human		name
156054165	CV2361179	single nucleotide variant	NM_001394154.1(RGS12):c.2977G>C (p.Glu993Gln)	not specified [RCV004216364]	uncertain significance	4	3422514	3422514	Human		name
156308123	CV2369868	single nucleotide variant	NM_001394154.1(RGS12):c.1927C>T (p.Arg643Cys)	not specified [RCV004208339]	uncertain significance	4	3342982	3342982	Human		name
156186385	CV2377962	single nucleotide variant	NM_001394154.1(RGS12):c.1561C>A (p.Pro521Thr)	not specified [RCV004230527]	uncertain significance	4	3317731	3317731	Human		name
156101347	CV2393015	single nucleotide variant	NM_001394154.1(RGS12):c.2717C>T (p.Thr906Ile)	not specified [RCV004242867]	uncertain significance	4	3417497	3417497	Human		name
329371088	CV2431864	single nucleotide variant	NM_001394154.1(RGS12):c.1409C>G (p.Ala470Gly)	not specified [RCV004255003]	uncertain significance	4	3317579	3317579	Human		name
329354819	CV2449085	single nucleotide variant	NM_001394154.1(RGS12):c.2188T>G (p.Ser730Ala)	not specified [RCV004264151]	uncertain significance	4	3414239	3414239	Human		name
329358515	CV2450342	single nucleotide variant	NM_001394154.1(RGS12):c.1070G>T (p.Arg357Leu)	not specified [RCV004271422]	uncertain significance	4	3317240	3317240	Human		name
329402013	CV2458046	single nucleotide variant	NM_001394154.1(RGS12):c.2921G>A (p.Cys974Tyr)	not specified [RCV004271606]	uncertain significance	4	3422458	3422458	Human		name
329398547	CV2471171	single nucleotide variant	NM_001394154.1(RGS12):c.2696C>T (p.Ser899Leu)	not specified [RCV004278418]	uncertain significance	4	3417476	3417476	Human		name
329381493	CV2471172	single nucleotide variant	NM_001394154.1(RGS12):c.2705G>T (p.Arg902Leu)	not specified [RCV004278419]	uncertain significance	4	3417485	3417485	Human		name
401721291	CV2673666	single nucleotide variant	NM_001394154.1(RGS12):c.1403G>C (p.Trp468Ser)	not specified [RCV004282397]	uncertain significance	4	3317573	3317573	Human		name
401743165	CV2687882	single nucleotide variant	NM_001394154.1(RGS12):c.2731A>C (p.Lys911Gln)	not specified [RCV004303184]	uncertain significance	4	3417511	3417511	Human		name
401762439	CV2696127	single nucleotide variant	NM_001394154.1(RGS12):c.2906C>T (p.Pro969Leu)	not specified [RCV004310188]	uncertain significance	4	3422443	3422443	Human		name
401726081	CV2699072	single nucleotide variant	NM_001394154.1(RGS12):c.1340C>T (p.Ser447Leu)	not specified [RCV004303586]	uncertain significance	4	3317510	3317510	Human		name
401751584	CV2708721	single nucleotide variant	NM_001394154.1(RGS12):c.2092G>C (p.Val698Leu)	not specified [RCV004307692]	uncertain significance	4	3414143	3414143	Human		name
401777032	CV2721577	single nucleotide variant	NM_001394154.1(RGS12):c.1351G>A (p.Gly451Ser)	not specified [RCV004316087]	uncertain significance	4	3317521	3317521	Human		name
401927862	CV2822364	single nucleotide variant	NM_001394154.1(RGS12):c.2390C>T (p.Ala797Val)	not provided [RCV003439219]	likely benign	4	3416084	3416084	Human		name
405715179	CV3309144	single nucleotide variant	NM_001394154.1(RGS12):c.1138C>T (p.Leu380Phe)	not specified [RCV004449083]	uncertain significance	4	3317308	3317308	Human		name
405715185	CV3309145	single nucleotide variant	NM_001394154.1(RGS12):c.1256G>T (p.Ser419Ile)	not specified [RCV004449084]	uncertain significance	4	3317426	3317426	Human		name
405715194	CV3309146	single nucleotide variant	NM_001394154.1(RGS12):c.1393G>A (p.Ala465Thr)	not specified [RCV004449085]	likely benign	4	3317563	3317563	Human		name
405715201	CV3309147	single nucleotide variant	NM_001394154.1(RGS12):c.1405G>A (p.Gly469Ser)	not specified [RCV004449086]	uncertain significance	4	3317575	3317575	Human		name
405715208	CV3309148	single nucleotide variant	NM_001394154.1(RGS12):c.1528G>A (p.Val510Met)	not specified [RCV004449087]	uncertain significance	4	3317698	3317698	Human		name
405715214	CV3309149	single nucleotide variant	NM_001394154.1(RGS12):c.1630C>T (p.Arg544Trp)	not specified [RCV004449088]	uncertain significance	4	3317800	3317800	Human		name
405715220	CV3309150	single nucleotide variant	NM_001394154.1(RGS12):c.1675G>T (p.Asp559Tyr)	not specified [RCV004449089]	uncertain significance	4	3317845	3317845	Human		name
405715228	CV3309151	single nucleotide variant	NM_001394154.1(RGS12):c.1777C>T (p.Pro593Ser)	not specified [RCV004449090]	uncertain significance	4	3317947	3317947	Human		name
405715242	CV3309153	single nucleotide variant	NM_001394154.1(RGS12):c.1790C>T (p.Ala597Val)	not specified [RCV004449092]	uncertain significance	4	3317960	3317960	Human		name
405715248	CV3309154	single nucleotide variant	NM_001394154.1(RGS12):c.1940G>A (p.Arg647Gln)	not specified [RCV004449093]	uncertain significance	4	3342995	3342995	Human		name
405715255	CV3309155	single nucleotide variant	NM_001394154.1(RGS12):c.2246A>T (p.Glu749Val)	not specified [RCV004449094]	uncertain significance	4	3414807	3414807	Human		name
405715262	CV3309156	single nucleotide variant	NM_001394154.1(RGS12):c.2300G>A (p.Arg767Gln)	not specified [RCV004449095]	uncertain significance	4	3415994	3415994	Human		name
405715277	CV3309158	single nucleotide variant	NM_001394154.1(RGS12):c.2747G>A (p.Gly916Glu)	not specified [RCV004449097]	uncertain significance	4	3417527	3417527	Human		name
405715284	CV3309159	single nucleotide variant	NM_001394154.1(RGS12):c.2840C>T (p.Ser947Leu)	not specified [RCV004449098]	uncertain significance	4	3422377	3422377	Human		name
407508078	CV3472795	single nucleotide variant	NM_001394154.1(RGS12):c.2255A>G (p.Asn752Ser)	not specified [RCV004671929]	uncertain significance	4	3414816	3414816	Human		name
407508081	CV3472796	single nucleotide variant	NM_001394154.1(RGS12):c.1091C>T (p.Thr364Met)	not specified [RCV004671930]	uncertain significance	4	3317261	3317261	Human		name
407508088	CV3472799	single nucleotide variant	NM_001394154.1(RGS12):c.2050G>A (p.Val684Ile)	not specified [RCV004671932]	uncertain significance	4	3414101	3414101	Human		name
407474214	CV3472802	single nucleotide variant	NM_001394154.1(RGS12):c.2791C>T (p.Arg931Cys)	not specified [RCV004662942]	uncertain significance	4	3420671	3420671	Human		name
407508092	CV3472807	single nucleotide variant	NM_001394154.1(RGS12):c.1219G>A (p.Asp407Asn)	not specified [RCV004671933]	uncertain significance	4	3317389	3317389	Human		name
407474235	CV3472808	single nucleotide variant	NM_001394154.1(RGS12):c.1354C>A (p.Pro452Thr)	not specified [RCV004662947]	uncertain significance	4	3317524	3317524	Human		name
597787988	CV3586290	single nucleotide variant	NM_001394154.1(RGS12):c.1309C>T (p.Arg437Trp)	not specified [RCV004855379]	uncertain significance	4	3317479	3317479	Human		name
597787996	CV3586292	single nucleotide variant	NM_001394154.1(RGS12):c.2104C>T (p.Arg702Trp)	not specified [RCV004855381]	uncertain significance	4	3414155	3414155	Human		name
597775668	CV3586293	single nucleotide variant	NM_001394154.1(RGS12):c.2389G>A (p.Ala797Thr)	not specified [RCV004852310]	uncertain significance	4	3416083	3416083	Human		name
597775672	CV3586294	single nucleotide variant	NM_001394154.1(RGS12):c.1465G>A (p.Ala489Thr)	not specified [RCV004852311]	uncertain significance	4	3317635	3317635	Human		name
597788004	CV3586296	single nucleotide variant	NM_001394154.1(RGS12):c.2686G>A (p.Ala896Thr)	not specified [RCV004855383]	uncertain significance	4	3417466	3417466	Human		name
597788008	CV3586298	single nucleotide variant	NM_001394154.1(RGS12):c.1207C>T (p.Arg403Cys)	not specified [RCV004855384]	uncertain significance	4	3317377	3317377	Human		name
597788010	CV3586299	single nucleotide variant	NM_001394154.1(RGS12):c.2387G>A (p.Arg796His)	not specified [RCV004855385]	uncertain significance	4	3416081	3416081	Human		name
597788018	CV3586305	single nucleotide variant	NM_001394154.1(RGS12):c.1390G>C (p.Gly464Arg)	not specified [RCV004855387]	uncertain significance	4	3317560	3317560	Human		name
597775695	CV3586306	single nucleotide variant	NM_001394154.1(RGS12):c.1939C>T (p.Arg647Trp)	not specified [RCV004852317]	uncertain significance	4	3342994	3342994	Human		name
597775699	CV3586307	single nucleotide variant	NM_001394154.1(RGS12):c.1493T>C (p.Leu498Pro)	not specified [RCV004852318]	uncertain significance	4	3317663	3317663	Human		name
597788022	CV3586308	single nucleotide variant	NM_001394154.1(RGS12):c.1816G>A (p.Ala606Thr)	not specified [RCV004855388]	uncertain significance	4	3317986	3317986	Human		name
597775701	CV3586309	single nucleotide variant	NM_001394154.1(RGS12):c.2981G>A (p.Arg994Gln)	not specified [RCV004852319]	uncertain significance	4	3422518	3422518	Human		name
597775705	CV3586311	single nucleotide variant	NM_001394154.1(RGS12):c.2035G>A (p.Asp679Asn)	not specified [RCV004852320]	uncertain significance	4	3414086	3414086	Human		name
597775709	CV3586312	single nucleotide variant	NM_001394154.1(RGS12):c.1562C>A (p.Pro521His)	not specified [RCV004852321]	uncertain significance	4	3317732	3317732	Human		name
597788035	CV3586314	single nucleotide variant	NM_001394154.1(RGS12):c.1498A>G (p.Lys500Glu)	not specified [RCV004855391]	uncertain significance	4	3317668	3317668	Human		name
597788037	CV3586315	single nucleotide variant	NM_001394154.1(RGS12):c.2845G>A (p.Ala949Thr)	not specified [RCV004855392]	uncertain significance	4	3422382	3422382	Human		name
597775713	CV3586317	single nucleotide variant	NM_001394154.1(RGS12):c.1778C>T (p.Pro593Leu)	not specified [RCV004852322]	uncertain significance	4	3317948	3317948	Human		name
598188805	CV3902534	single nucleotide variant	NM_001394154.1(RGS12):c.2030G>T (p.Gly677Val)	not specified [RCV005266628]	uncertain significance	4	3414081	3414081	Human		name
598188827	CV3902537	single nucleotide variant	NM_001394154.1(RGS12):c.2170G>A (p.Val724Ile)	not specified [RCV005266631]	uncertain significance	4	3414221	3414221	Human		name
598188855	CV3902541	single nucleotide variant	NM_001394154.1(RGS12):c.1817C>T (p.Ala606Val)	not specified [RCV005266635]	uncertain significance	4	3317987	3317987	Human		name
598188877	CV3902544	single nucleotide variant	NM_001394154.1(RGS12):c.2143T>A (p.Ser715Thr)	not specified [RCV005266638]	uncertain significance	4	3414194	3414194	Human		name
598188884	CV3902545	single nucleotide variant	NM_001394154.1(RGS12):c.1642T>C (p.Cys548Arg)	not specified [RCV005266639]	uncertain significance	4	3317812	3317812	Human		name
598188891	CV3902546	single nucleotide variant	NM_001394154.1(RGS12):c.1684G>A (p.Asp562Asn)	not specified [RCV005266640]	uncertain significance	4	3317854	3317854	Human		name
155962984	CV2197706	single nucleotide variant	NM_001394154.1(RGS12):c.3166G>A (p.Val1056Ile)	not specified [RCV004074912]	uncertain significance	4	3423573	3423573	Human		name
156095195	CV2213563	single nucleotide variant	NM_001394154.1(RGS12):c.3926C>T (p.Ala1309Val)	not specified [RCV004087515]	uncertain significance	4	3430767	3430767	Human		name
156327317	CV2217254	single nucleotide variant	NM_001394154.1(RGS12):c.3868C>T (p.Pro1290Ser)	not specified [RCV004087703]	uncertain significance	4	3430709	3430709	Human		name
156380341	CV2218104	single nucleotide variant	NM_001394154.1(RGS12):c.4009G>A (p.Val1337Met)	not specified [RCV004086534]	uncertain significance	4	3430850	3430850	Human		name
156234868	CV2223994	single nucleotide variant	NM_001394154.1(RGS12):c.3815C>A (p.Ser1272Tyr)	not specified [RCV004094245]	uncertain significance	4	3430656	3430656	Human		name
155984242	CV2241097	single nucleotide variant	NM_001394154.1(RGS12):c.4331C>A (p.Ala1444Asp)	not specified [RCV004104133]	uncertain significance	4	3439671	3439671	Human		name
156181420	CV2246227	single nucleotide variant	NM_001394154.1(RGS12):c.3763T>C (p.Ser1255Pro)	not specified [RCV004107686]	likely benign	4	3430604	3430604	Human		name
156314231	CV2257127	single nucleotide variant	NM_001394154.1(RGS12):c.3410C>T (p.Thr1137Met)	not specified [RCV004123086]	uncertain significance	4	3428168	3428168	Human		name
155986763	CV2282672	single nucleotide variant	NM_001394154.1(RGS12):c.3291G>C (p.Gln1097His)	not specified [RCV004135221]	uncertain significance	4	3425520	3425520	Human		name
155942706	CV2298278	single nucleotide variant	NM_001394154.1(RGS12):c.3026G>A (p.Gly1009Glu)	not specified [RCV004160192]	uncertain significance	4	3422563	3422563	Human		name
156187416	CV2302783	single nucleotide variant	NM_001394154.1(RGS12):c.3914C>T (p.Pro1305Leu)	not specified [RCV004162701]	uncertain significance	4	3430755	3430755	Human		name
155961696	CV2311941	single nucleotide variant	NM_001394154.1(RGS12):c.3397A>C (p.Asn1133His)	not specified [RCV004170763]	uncertain significance	4	3428155	3428155	Human		name
155960652	CV2314051	single nucleotide variant	NM_001394154.1(RGS12):c.4192G>A (p.Gly1398Arg)	not specified [RCV004164330]	uncertain significance	4	3439532	3439532	Human		name
156175764	CV2317283	single nucleotide variant	NM_001394154.1(RGS12):c.4111C>T (p.Pro1371Ser)	not specified [RCV004178774]	uncertain significance	4	3430952	3430952	Human		name
156284328	CV2317533	single nucleotide variant	NM_001394154.1(RGS12):c.4015G>A (p.Glu1339Lys)	not specified [RCV004172489]	uncertain significance	4	3430856	3430856	Human		name
155977922	CV2321300	single nucleotide variant	NM_001394154.1(RGS12):c.3637G>T (p.Asp1213Tyr)	not specified [RCV004177313]	uncertain significance	4	3430478	3430478	Human		name
156053300	CV2333282	single nucleotide variant	NM_001394154.1(RGS12):c.3869C>A (p.Pro1290His)	not specified [RCV004197031]	uncertain significance	4	3430710	3430710	Human		name
156245913	CV2347274	single nucleotide variant	NM_001394154.1(RGS12):c.3860C>T (p.Thr1287Met)	not specified [RCV004204736]	uncertain significance	4	3430701	3430701	Human		name
155926076	CV2348608	single nucleotide variant	NM_001394154.1(RGS12):c.3752G>A (p.Arg1251Gln)	not specified [RCV004195834]	uncertain significance	4	3430593	3430593	Human		name
156143556	CV2358586	single nucleotide variant	NM_001394154.1(RGS12):c.3170C>T (p.Thr1057Met)	not specified [RCV004207466]	uncertain significance	4	3423577	3423577	Human		name
156201754	CV2392517	single nucleotide variant	NM_001394154.1(RGS12):c.3379G>A (p.Val1127Ile)	not specified [RCV004245385]	uncertain significance	4	3428137	3428137	Human		name
156222996	CV2394805	single nucleotide variant	NM_001394154.1(RGS12):c.4318A>G (p.Ser1440Gly)	not specified [RCV004234472]	uncertain significance	4	3439658	3439658	Human		name
329398452	CV2464594	single nucleotide variant	NM_001394154.1(RGS12):c.3151A>G (p.Lys1051Glu)	not specified [RCV004278286]	uncertain significance	4	3423558	3423558	Human		name
401722360	CV2676954	single nucleotide variant	NM_001394154.1(RGS12):c.3016C>G (p.Leu1006Val)	not specified [RCV004293556]	uncertain significance	4	3422553	3422553	Human		name
401761233	CV2689074	single nucleotide variant	NM_001394154.1(RGS12):c.4166T>C (p.Val1389Ala)	not specified [RCV004305844]	uncertain significance	4	3439506	3439506	Human		name
401746902	CV2692013	single nucleotide variant	NM_001394154.1(RGS12):c.3761C>T (p.Ala1254Val)	not specified [RCV004301739]	uncertain significance	4	3430602	3430602	Human		name
401769658	CV2731511	single nucleotide variant	NM_001394154.1(RGS12):c.3868C>G (p.Pro1290Ala)	not specified [RCV004330862]	uncertain significance	4	3430709	3430709	Human		name
401746606	CV2731877	single nucleotide variant	NM_001394154.1(RGS12):c.3734G>C (p.Ser1245Thr)	not specified [RCV004333122]	uncertain significance	4	3430575	3430575	Human		name
401884914	CV2771050	single nucleotide variant	NM_001394154.1(RGS12):c.3758G>C (p.Ser1253Thr)	not specified [RCV004346061]	uncertain significance	4	3430599	3430599	Human		name
401886730	CV2771387	single nucleotide variant	NM_001394154.1(RGS12):c.3695C>G (p.Pro1232Arg)	not specified [RCV004348143]	uncertain significance	4	3430536	3430536	Human		name
405715296	CV3309161	single nucleotide variant	NM_001394154.1(RGS12):c.3083G>A (p.Arg1028His)	not specified [RCV004449100]	uncertain significance	4	3422954	3422954	Human		name
405715335	CV3309166	single nucleotide variant	NM_001394154.1(RGS12):c.3751C>G (p.Arg1251Gly)	not specified [RCV004449105]	uncertain significance	4	3430592	3430592	Human		name
405715342	CV3309167	single nucleotide variant	NM_001394154.1(RGS12):c.3832G>C (p.Ala1278Pro)	not specified [RCV004449106]	uncertain significance	4	3430673	3430673	Human		name
405715350	CV3309168	single nucleotide variant	NM_001394154.1(RGS12):c.3868C>A (p.Pro1290Thr)	not specified [RCV004449107]	uncertain significance	4	3430709	3430709	Human		name
405715360	CV3309170	single nucleotide variant	NM_001394154.1(RGS12):c.3917T>G (p.Val1306Gly)	not specified [RCV004449109]	uncertain significance	4	3430758	3430758	Human		name
405715367	CV3309171	single nucleotide variant	NM_001394154.1(RGS12):c.3919T>A (p.Ser1307Thr)	not specified [RCV004449110]	uncertain significance	4	3430760	3430760	Human		name
405715375	CV3309172	single nucleotide variant	NM_001394154.1(RGS12):c.3925G>A (p.Ala1309Thr)	not specified [RCV004449111]	uncertain significance	4	3430766	3430766	Human		name
405715384	CV3309173	single nucleotide variant	NM_001394154.1(RGS12):c.4022C>A (p.Thr1341Asn)	not specified [RCV004449112]	uncertain significance	4	3430863	3430863	Human		name
405715397	CV3309175	single nucleotide variant	NM_001394154.1(RGS12):c.4321G>A (p.Ala1441Thr)	not specified [RCV004449114]	uncertain significance	4	3439661	3439661	Human		name
405715402	CV3309176	single nucleotide variant	NM_001394154.1(RGS12):c.4339G>A (p.Val1447Ile)	not specified [RCV004449115]	uncertain significance	4	3439679	3439679	Human		name
407460457	CV3472797	single nucleotide variant	NM_001394154.1(RGS12):c.3187G>A (p.Val1063Met)	not specified [RCV004658459]	uncertain significance	4	3423594	3423594	Human		name
407474223	CV3472804	single nucleotide variant	NM_001394154.1(RGS12):c.3095G>A (p.Arg1032His)	not specified [RCV004662944]	uncertain significance	4	3422966	3422966	Human		name
407474226	CV3472805	single nucleotide variant	NM_001394154.1(RGS12):c.3943C>G (p.Gln1315Glu)	not specified [RCV004662945]	uncertain significance	4	3430784	3430784	Human		name
407474231	CV3472806	single nucleotide variant	NM_001394154.1(RGS12):c.3118G>T (p.Val1040Phe)	not specified [RCV004662946]	uncertain significance	4	3423525	3423525	Human		name
407474240	CV3472809	single nucleotide variant	NM_001394154.1(RGS12):c.3521T>C (p.Ile1174Thr)	not specified [RCV004662948]	uncertain significance	4	3428667	3428667	Human		name
597775717	CV3586318	single nucleotide variant	NM_001394154.1(RGS12):c.4196G>A (p.Arg1399Gln)	not specified [RCV004852323]	likely benign	4	3439536	3439536	Human		name
598188820	CV3902536	single nucleotide variant	NM_001394154.1(RGS12):c.3487C>T (p.Arg1163Trp)	not specified [RCV005266630]	uncertain significance	4	3428633	3428633	Human		name
598188841	CV3902539	single nucleotide variant	NM_001394154.1(RGS12):c.3782G>C (p.Trp1261Ser)	not specified [RCV005266633]	uncertain significance	4	3430623	3430623	Human		name
598188863	CV3902542	single nucleotide variant	NM_001394154.1(RGS12):c.4022C>T (p.Thr1341Ile)	not specified [RCV005266636]	uncertain significance	4	3430863	3430863	Human		name

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